Literature DB >> 1592027

Unilateral opercular macrogyria and benign childhood epilepsy with centrotemporal (rolandic) spikes: report of a case.

G Ambrosetto1.   

Abstract

An 18-year-old mentally normal epileptic boy had frequent left brachiofacial or unilateral motor seizures which started at age 4 years and ceased 10 years later. Seizures were exclusively sleep-related. No relapse followed antiepileptic drug (AED) discontinuation. Left arm slight paresis and left hand astereognosia occurred at age 10 years. Awake EEGs showed persistent right rolandic discharges increased by sleep. Somatosensory evoked potentials (SEPs) were giant with left median nerve stimulation. Computed tomography (CT) and magnetic resonance imaging (MRI) disclosed right opercular macrogyria. We suggest that the structural brain lesion was causally related to his "idiopathic" partial epilepsy. Similar case reports and pathologic studies will elucidate the morphologic substrate of the underlying functional disorder in idiopathic partial epilepsies.

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Year:  1992        PMID: 1592027     DOI: 10.1111/j.1528-1157.1992.tb01699.x

Source DB:  PubMed          Journal:  Epilepsia        ISSN: 0013-9580            Impact factor:   5.864


  1 in total

1.  Benign epilepsy of childhood with centrotemporal spikes and unilateral developmental opercular dysplasia.

Authors:  P Iannetti; U Raucci; L A Basile; A Spalice; P Parisi; G Fariello; C Imperato
Journal:  Childs Nerv Syst       Date:  1994-05       Impact factor: 1.475

  1 in total

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